J. M. Connor - Concepedia

Author

J. M. Connor

Also Known As

J CONNOR, J M Connor, J Michael Connor, J. Connor, J. M. CONNOR, J. M. Connor, J. M. O Connor, J. MICHAEL CONNOR, J. Michael CONNOR, J. Michael Connor

137

Publications

8.1K

Citations

H-Index

123

Concepts

All Affiliations

Institute of Genetics University of Glasgow Western Infirmary Southbank Centre Institute of Genetics

About

J. M. Connor is an author at Institute of Genetics specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	46	4.8K
2	Public Health	10	10	1.1K
3	Natural Sciences	5	5	70
4	Health Sciences	2	2	41
5	Anatomy	1	1	50

J. M. Connor

Publications

7.6K

Citations

H-Index

Page 1

	Year	Citations
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva Eileen M. Shore, Meiqi Xu, George Feldman, Nature Genetics Recurrent MutationFibrosisSignal TransductionBmp TypeSporadic Fibrodysplasia Ossificans	2006	1.2K
EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9 Alan Fryer, J. M. Connor, S. Povey, The Lancet CytogeneticsGenetic DisorderGeneticsPathologyTuberous Sclerosis	1987	514
Early Pregnancy Levels of Pregnancy-Associated Plasma Protein A and the Risk of Intrauterine Growth Restriction, Premature Birth, Preeclampsia, and Stillbirth Gordon C. S. Smith, Emily Stenhouse, Jennifer A. Crossley, The Journal of Clinical Endocrinology & Metabolism FertilityIntrauterine Growth RestrictionGynecologyEarly Pregnancy LevelsHigh-risk Pregnancy	2002	466
Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1 Frederick S. Kaplan, Meiqi Xu, Petra Seemann, Human Mutation	2008	436
Fibrodysplasia ossificans progressiva. The clinical features and natural history of 34 patients J. M. Connor, DA Evans Journal of Bone and Joint Surgery - British Volume Thumb HypoplasiaFibrosisMedical TreatmentMusculoskeletal DisordersOsteopathy	1982	362
Abnormalities of glucocorticoid metabolism and the renin???angiotensin system: a four-corners approach to the identification of genetic determinants of blood pressure Graham Watt, Stephen Harrap, Christopher Foy, Journal of Hypertension	1992	304
Genetic aspects of tuberous sclerosis in the west of Scotland. Julian R. Sampson, S J Scahill, J Stephenson, Journal of Medical Genetics Developmental AnomalyInfertilityMendelian DisorderSingle New MutationGenetic Disorder	1989	227
Circulating Angiogenic Factors in Early Pregnancy and the Risk of Preeclampsia, Intrauterine Growth Restriction, Spontaneous Preterm Birth, and Stillbirth Gordon C. S. Smith, Jennifer A. Crossley, David A. Aitken, Obstetrics and Gynecology	2007	218
Dimeric Inhibin A as a Marker for Down's Syndrome in Early Pregnancy David A. Aitken, Euan M. Wallace, Jennifer A. Crossley, New England Journal of Medicine	1996	182
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition Edward G. D. Tuddenham, R. Schwaab, J. Seehafer, Nucleic Acids Research Second EditionF8 GeneInversional EventsGeneticsPathogenesis	1994	148

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